The answer is Klinefelter syndrome.
Nondisjunction disorders are conditions resulting from an unbalanced distribution of chromosomes. In the case of Klinefelter syndrome, the sex chromosomes are affected. Rather than having an XX for female or an XY for male people with Klinefelters have either XXY or XYY.
Answer:
The type of mutation that causes this translation error is called deletion. Deletion occurs when a section of a DNA is deleted or lost. In cystic fibrosis, three nucleotides are deleted that results in the lost of phenylalanine
Pangaea started to break apart.
The patter of inheritance would support the hypothesis that the trait being studied is a recessive sex- linked trait found on the X chromosome "The trait is mostly expressed in males who have a maternal grandfather with the trait."
Explanation:
A pedigree chart is a illustration that displays the existence and arrival of phenotypes of a specific genetic factor or organism and its families from one group to the next, most usually individuals, show dogs, and race horses. A pedigree chart displays a family tree, and shows the members of the family who are affected by a genetic trait. This chart shows four generations of a family with four individuals who are affected by a form of colorblindness. Circles represent females and squares represent males.
